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Clinical Case Reports|July 26, 2021
Prenatal cases with rare RIT1 variants causing severe fetal hydrops and deathIeva Miceikaite, Geske Sidsel Bak, Martin Jakob Larsen, et al.Nature Communications|August 23, 2025
Deep genome sequencing reveals extensive genetic heterogeneity in early human placentasIeva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen, et al.Molecular Genetics & Genomic Medicine|October 15, 2020
Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic TelangiectasiaKatrine S Aagaard, Klaus Brusgaard, Ieva Miceikaite, et al.Prenatal Diagnosis|June 25, 2023
Comprehensive prenatal diagnostics: Exome versus genome sequencingIeva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen, et al.Breast Cancer Research : BCR|January 9, 2024
Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variantInes Block, Àngels Mateu-Regué, Thi Tuyet Nhu Do, et al.Clinical Genetics|July 23, 2021
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype-phenotype spectrum and functional impact on GPI-anchored proteinsSmrithi Salian, Marcello Scala, Thi Tuyet Mai Nguyen, et al.Pageof 1